Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy

Author:

Wang Hongyan1ORCID,Li Xia1,Yang Kaiyue1,Guo Fanfan1,Wang Xiaona1,Zhao Ziyan1,Jia Yanju1,Gao Fan2,Bai Guiqin3

Affiliation:

1. Department of Obstetrics and Gynecology the First Affiliated Hospital of Xi'an Jiaotong University Xi'an China

2. Clinical Research Center the First Affiliated Hospital of Xi'an Jiaotong University Xi'an China

3. Gene Joint Laboratory the First Affiliated Hospital of Xi'an Jiaotong University Xi'an China

Abstract

AbstractThere is a growing body of evidence that innate immunity also plays an important role in the progression of hepatitis B virus (HBV) infection. However, there is less study on systematically elucidating the characteristics of innate immunity in HBV‐infected pregnant women. We compared the features of peripheral blood mononuclear cells in three healthy pregnant women and three HBV‐infected pregnant women by single‐cell RNA sequencing. 10 DEGs were detected between groups and monocytes were the main expression source of most of the DEGs, which involved in the inflammatory response, apoptosis and immune regulation. Meanwhile, qPCR and ELISA were performed to verify above genes. Monocytes displayed immune response defect, reflecting poor ability of response to IFN. In addition, eight clusters were identified in monocytes. We identified molecular drivers in monocytes subpopulations.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes were featured with different gene expression pattern and biological function.TNFSF10+ monocytes and MT1G+ monocytes were characterized by high levels of inflammation response.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes showed decreased response to IFN. Our results dissects alterations in monocytes related to the immune response of HBV‐infected pregnant women and provides a rich resource for fully understanding immunopathogenesis and developing effective preventing HBV intrauterine infection strategies.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

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